Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

75 records found for search term Sgip1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156090733CV2256530single nucleotide variantNM_032291.4(SGIP1):c.4A>G (p.Met2Val)not specified [RCV004118731]uncertain significance16653436266534362Humanname
405706639CV3321600single nucleotide variantNM_032291.4(SGIP1):c.22C>T (p.Arg8Cys)not specified [RCV004447874]uncertain significance16662585866625858Humanname
156331243CV2218134single nucleotide variantNM_032291.4(SGIP1):c.41G>C (p.Gly14Ala)not specified [RCV004086561]uncertain significance16662587766625877Humanname
155983048CV2239945single nucleotide variantNM_032291.4(SGIP1):c.40G>A (p.Gly14Arg)not specified [RCV004110746]uncertain significance16662587666625876Humanname
401740719CV2681508single nucleotide variantNM_032291.4(SGIP1):c.46C>T (p.Arg16Trp)not specified [RCV004292042]uncertain significance16662588266625882Humanname
405706686CV3321607single nucleotide variantNM_032291.4(SGIP1):c.89G>C (p.Arg30Thr)not specified [RCV004447881]uncertain significance16663308466633084Humanname
597673052CV3595721single nucleotide variantNM_032291.4(SGIP1):c.68A>G (p.Asp23Gly)not specified [RCV004856638]uncertain significance16662590466625904Humanname
401868490CV2767252single nucleotide variantNM_032291.4(SGIP1):c.115G>A (p.Glu39Lys)not specified [RCV004349426]uncertain significance16663595966635959Humanname
405706614CV3321596single nucleotide variantNM_032291.4(SGIP1):c.205G>A (p.Ala69Thr)not specified [RCV004447870]uncertain significance16663981066639810Humanname
407490189CV3484079single nucleotide variantNM_032291.4(SGIP1):c.149G>A (p.Arg50His)not specified [RCV004666228]uncertain significance16663599366635993Humanname
597672987CV3595713single nucleotide variantNM_032291.4(SGIP1):c.206C>T (p.Ala69Val)not specified [RCV004856630]uncertain significance16663981166639811Humanname
597673013CV3595716single nucleotide variantNM_032291.4(SGIP1):c.165A>T (p.Lys55Asn)not specified [RCV004856633]uncertain significance16663600966636009Humanname
598166848CV3921220single nucleotide variantNM_032291.4(SGIP1):c.125A>G (p.Tyr42Cys)not specified [RCV005283731]uncertain significance16663596966635969Humanname
15180460CV707498single nucleotide variantNM_032291.4(SGIP1):c.1290G>A (p.Ser430=)not provided [RCV000974159]benign16668234466682344Humanname
156142495CV2208536single nucleotide variantNM_032291.4(SGIP1):c.811C>T (p.Pro271Ser)not specified [RCV004091066]uncertain significance16667974966679749Humanname
156334288CV2230902single nucleotide variantNM_032291.4(SGIP1):c.479G>T (p.Ser160Ile)not specified [RCV004092374]uncertain significance16666753766667537Humanname
155917802CV2275068single nucleotide variantNM_032291.4(SGIP1):c.892G>T (p.Val298Leu)not specified [RCV004136887]uncertain significance16668194666681946Humanname
156107092CV2303885single nucleotide variantNM_032291.4(SGIP1):c.911T>C (p.Val304Ala)not specified [RCV004168169]uncertain significance16668196566681965Humanname
156075742CV2350900single nucleotide variantNM_032291.4(SGIP1):c.724C>T (p.Pro242Ser)not specified [RCV004211737]uncertain significance16667708166677081Humanname
156186199CV2377931single nucleotide variantNM_032291.4(SGIP1):c.476G>A (p.Arg159His)not specified [RCV004230497]uncertain significance16666753466667534Humanname
401893944CV2770141single nucleotide variantNM_032291.4(SGIP1):c.952A>G (p.Thr318Ala)not specified [RCV004356042]uncertain significance16668200666682006Humanname
401887320CV2773366single nucleotide variantNM_032291.4(SGIP1):c.733A>G (p.Thr245Ala)not specified [RCV004354016]uncertain significance16667709066677090Humanname
401898840CV2782747single nucleotide variantNM_032291.4(SGIP1):c.670T>G (p.Trp224Gly)not specified [RCV004359747]uncertain significance16667702766677027Humanname
401895178CV2789752single nucleotide variantNM_032291.4(SGIP1):c.389T>C (p.Leu130Pro)not specified [RCV004361866]uncertain significance16664364966643649Humanname
405706647CV3321601single nucleotide variantNM_032291.4(SGIP1):c.359A>G (p.Lys120Arg)not specified [RCV004447875]uncertain significance16664361966643619Humanname
405706667CV3321604single nucleotide variantNM_032291.4(SGIP1):c.505T>C (p.Ser169Pro)not specified [RCV004447878]uncertain significance16667101666671016Humanname
405706675CV3321605single nucleotide variantNM_032291.4(SGIP1):c.533G>C (p.Arg178Pro)not specified [RCV004447879]uncertain significance16667196866671968Humanname
405706681CV3321606single nucleotide variantNM_032291.4(SGIP1):c.838G>A (p.Val280Ile)not specified [RCV004447880]likely benign16668189266681892Humanname
405706695CV3321608single nucleotide variantNM_032291.4(SGIP1):c.953C>T (p.Thr318Ile)not specified [RCV004447882]uncertain significance16668200766682007Humanname
407492672CV3484080single nucleotide variantNM_032291.4(SGIP1):c.448C>G (p.Pro150Ala)not specified [RCV004667220]uncertain significance16664370866643708Humanname
407490192CV3484081single nucleotide variantNM_032291.4(SGIP1):c.650T>C (p.Leu217Pro)not specified [RCV004666229]uncertain significance16667700766677007Humanname
407490195CV3484084single nucleotide variantNM_032291.4(SGIP1):c.535T>C (p.Ser179Pro)not specified [RCV004666230]uncertain significance16667197066671970Humanname
407492684CV3484087single nucleotide variantNM_032291.4(SGIP1):c.830C>A (p.Ala277Asp)not specified [RCV004667223]uncertain significance16668188466681884Humanname
597672997CV3595714single nucleotide variantNM_032291.4(SGIP1):c.657T>A (p.Asp219Glu)not specified [RCV004856631]uncertain significance16667701466677014Humanname
597673057CV3595722single nucleotide variantNM_032291.4(SGIP1):c.766G>T (p.Val256Leu)not specified [RCV004856639]uncertain significance16667970466679704Humanname
597673065CV3595724single nucleotide variantNM_032291.4(SGIP1):c.871T>G (p.Leu291Val)not specified [RCV004856640]uncertain significance16668192566681925Humanname
598166855CV3921221single nucleotide variantNM_032291.4(SGIP1):c.500A>T (p.Asn167Ile)not specified [RCV005283732]uncertain significance16667101166671011Humanname
156235707CV2245454single nucleotide variantNM_032291.4(SGIP1):c.1115C>G (p.Ser372Trp)not specified [RCV004109234]uncertain significance16668216966682169Humanname
156364314CV2271891single nucleotide variantNM_032291.4(SGIP1):c.1699A>T (p.Thr567Ser)not specified [RCV004130984]uncertain significance16671936266719362Humanname
155917537CV2274915single nucleotide variantNM_032291.4(SGIP1):c.1448G>A (p.Arg483Lys)not specified [RCV004134978]uncertain significance16669019466690194Humanname
156255961CV2277547single nucleotide variantNM_032291.4(SGIP1):c.1003T>C (p.Ser335Pro)not specified [RCV004145235]uncertain significance16668205766682057Humanname
155929351CV2356778single nucleotide variantNM_032291.4(SGIP1):c.2266A>T (p.Ile756Phe)not specified [RCV004202121]uncertain significance16674068966740689Humanname
156385494CV2364480single nucleotide variantNM_032291.4(SGIP1):c.1602C>A (p.Asp534Glu)not specified [RCV004217350]uncertain significance16669546566695465Humanname
156307341CV2369685single nucleotide variantNM_032291.4(SGIP1):c.1199C>A (p.Pro400His)not specified [RCV004215085]uncertain significance16668225366682253Humanname
156214280CV2385907single nucleotide variantNM_032291.4(SGIP1):c.1545G>C (p.Leu515Phe)not specified [RCV004226945]uncertain significance16669029166690291Humanname
329363153CV2467142single nucleotide variantNM_032291.4(SGIP1):c.1088C>T (p.Pro363Leu)not specified [RCV004282866]uncertain significance16668214266682142Humanname
401736033CV2689240single nucleotide variantNM_032291.4(SGIP1):c.1187C>A (p.Thr396Lys)not specified [RCV004306084]uncertain significance16668224166682241Humanname
401737931CV2700826single nucleotide variantNM_032291.4(SGIP1):c.1069C>T (p.Pro357Ser)not specified [RCV004307104]uncertain significance16668212366682123Humanname
401732958CV2702309single nucleotide variantNM_032291.4(SGIP1):c.1919C>G (p.Ala640Gly)not specified [RCV004314636]uncertain significance16673376866733768Humanname
401896505CV2780874single nucleotide variantNM_032291.4(SGIP1):c.2110C>G (p.Arg704Gly)not specified [RCV004354421]uncertain significance16673941366739413Humanname
405706566CV3321590single nucleotide variantNM_032291.4(SGIP1):c.1073C>T (p.Thr358Ile)not specified [RCV004447864]uncertain significance16668212766682127Humanname
405706573CV3321591single nucleotide variantNM_032291.4(SGIP1):c.1125T>G (p.Asn375Lys)not specified [RCV004447865]uncertain significance16668217966682179Humanname
405706581CV3321592single nucleotide variantNM_032291.4(SGIP1):c.1579C>A (p.Gln527Lys)not specified [RCV004447866]uncertain significance16669544266695442Humanname
405706589CV3321593single nucleotide variantNM_032291.4(SGIP1):c.1841G>A (p.Arg614Gln)not specified [RCV004447867]uncertain significance16672936266729362Humanname
405706595CV3321594single nucleotide variantNM_032291.4(SGIP1):c.2000C>T (p.Thr667Ile)not specified [RCV004447868]uncertain significance16673384966733849Humanname
405706601CV3321595single nucleotide variantNM_032291.4(SGIP1):c.2047A>G (p.Ile683Val)not specified [RCV004447869]uncertain significance16673935066739350Humanname
405706620CV3321597single nucleotide variantNM_032291.4(SGIP1):c.2110C>T (p.Arg704Cys)not specified [RCV004447871]uncertain significance16673941366739413Humanname
405706627CV3321598single nucleotide variantNM_032291.4(SGIP1):c.2135A>T (p.Asp712Val)not specified [RCV004447872]uncertain significance16673943866739438Humanname
405707206CV3321599single nucleotide variantNM_032291.4(SGIP1):c.2275A>C (p.Ile759Leu)not specified [RCV004447873]uncertain significance16674069866740698Humanname
407492676CV3484082single nucleotide variantNM_032291.4(SGIP1):c.1456A>G (p.Ser486Gly)not specified [RCV004667221]uncertain significance16669020266690202Humanname
407492680CV3484083single nucleotide variantNM_032291.4(SGIP1):c.2144C>T (p.Thr715Met)not specified [RCV004667222]uncertain significance16673944766739447Humanname
407490199CV3484085single nucleotide variantNM_032291.4(SGIP1):c.2057C>T (p.Thr686Ile)not specified [RCV004666231]uncertain significance16673936066739360Humanname
407490202CV3484086single nucleotide variantNM_032291.4(SGIP1):c.1460C>T (p.Pro487Leu)not specified [RCV004666232]uncertain significance16669020666690206Humanname
597672978CV3595712single nucleotide variantNM_032291.4(SGIP1):c.1228A>G (p.Thr410Ala)not specified [RCV004856629]uncertain significance16668228266682282Humanname
597673006CV3595715single nucleotide variantNM_032291.4(SGIP1):c.1913A>G (p.Asn638Ser)not specified [RCV004856632]uncertain significance16673376266733762Humanname
597673479CV3595717single nucleotide variantNM_032291.4(SGIP1):c.1750G>A (p.Val584Ile)not specified [RCV004856634]uncertain significance16672927166729271Humanname
597673028CV3595718single nucleotide variantNM_032291.4(SGIP1):c.1118C>T (p.Pro373Leu)not specified [RCV004856635]uncertain significance16668217266682172Humanname
597673035CV3595719single nucleotide variantNM_032291.4(SGIP1):c.1927A>G (p.Lys643Glu)not specified [RCV004856636]uncertain significance16673377666733776Humanname
597673042CV3595720single nucleotide variantNM_032291.4(SGIP1):c.2045G>A (p.Gly682Asp)not specified [RCV004856637]uncertain significance16673934866739348Humanname
597673072CV3595725single nucleotide variantNM_032291.4(SGIP1):c.1432G>C (p.Val478Leu)not specified [RCV004856641]uncertain significance16668926466689264Humanname
598166826CV3921216single nucleotide variantNM_032291.4(SGIP1):c.1591G>A (p.Val531Ile)not specified [RCV005283727]uncertain significance16669545466695454Humanname
598166832CV3921217single nucleotide variantNM_032291.4(SGIP1):c.1301C>T (p.Pro434Leu)not specified [RCV005283728]uncertain significance16668235566682355Humanname
598166843CV3921219single nucleotide variantNM_032291.4(SGIP1):c.1229C>G (p.Thr410Ser)not specified [RCV005283730]uncertain significance16668228366682283Humanname
598198605CV3921222single nucleotide variantNM_032291.4(SGIP1):c.2258T>C (p.Leu753Ser)not specified [RCV005268271]uncertain significance16674068166740681Humanname
598198612CV3921223single nucleotide variantNM_032291.4(SGIP1):c.1734C>A (p.Asp578Glu)not specified [RCV005268272]uncertain significance16671939766719397Humanname